JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB145582

Atropine, mAChR antagonist

Be the first to review this product! Submit a review

|

(4 Publications)

MW 289.4 Da, Purity >98%. Potent, competitive, non-selective mAChR antagonist (IC50 = 2.5 nM). Induces mydriasis. Shows antimuscarinic and anticholinergic effects in vivo. Orally active.
1 Images
Chemical Structure - Atropine, mAChR antagonist (AB145582)
  • Chemical Structure

Lab

Chemical Structure - Atropine, mAChR antagonist (AB145582)

2D chemical structure image of ab145582, Atropine, mAChR antagonist

Key facts

CAS number

51-55-8

Purity

>98%

Form

Solid

form

Source

Solanaceae sp.

Molecular weight

289.4 Da

Molecular formula

C<sub>1</sub><sub>7</sub>H<sub>2</sub><sub>3</sub>NO<sub>3</sub>

PubChem

3661

Nature

Native

Solubility

Soluble in water to 5 mM

Biochemical name

L-Hyoscyamine

Biological description

Potent, competitive, non-selective mAChR antagonist (IC50 = 2.5 nM). Induces mydriasis. Shows antimuscarinic and anticholinergic effects in vivo. Orally active.

Canonical smiles

CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3

InChi

InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3

InChiKey

RKUNBYITZUJHSG-UHFFFAOYSA-N

IUPAC Name

(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate

Properties and storage information

Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
Ambient
Appropriate long-term storage conditions
Ambient
Storage information
The product can be stored for up to 12 months

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Muscarinic Acetylcholine Receptor M3 also known as CHRM3 or M3 receptor plays an important role in various physiological processes. This receptor is part of the G-protein coupled receptor family and binds acetylcholine. The mass of CHRM3 is around 65 kDa. CHRM3 is widely expressed in various tissues including smooth muscle exocrine glands and in some cases the central nervous system. This extensive expression indicates its significance in multiple bodily functions.
Biological function summary

CHRM3 mediates cellular responses such as smooth muscle contraction and glandular secretion. It operates as part of a larger receptor complex that facilitates the signal transduction process. When acetylcholine binds to CHRM3 it activates downstream signaling pathways involving various intracellular messengers. This activation influences activities such as bronchoconstriction and salivation emphasizing the importance of M3 receptor in autonomic nervous system regulation.

Pathways

Studies show that CHRM3 engages with the inositol phospholipid-calcium signaling pathway. This pathway mobilizes calcium from intracellular stores working together with proteins like G-proteins and protein kinase C. These interactions lead to physiological effects such as muscle contraction and secretion. Moreover CHRM3 links with the MAPK/ERK pathway conveying signals that influence cell growth and differentiation. The intertwining of these pathways highlights CHRM3’s role in regulating key cellular functions.

CHRM3’s malfunction associates with asthma and chronic obstructive pulmonary disease (COPD). Dysregulated CHRM3 signaling can exacerbate symptoms involving bronchoconstriction and mucus secretion. Furthermore CHRM3 connects to proteins affecting airway smooth muscle cells intensifying disease conditions. Its relevance in exocrine gland regulation also implicates CHRM3 in conditions like Sjögren's syndrome where it may impact salivary and lacrimal gland secretion. Understanding these connections aids in developing targeted therapies for these ailments.

Product protocols

Publications (4)

Recent publications for all applications. Explore the full list and refine your search

The Journal of neuroscience : the official journal of the Society for Neuroscience 43:722-735 PubMed36535767

2022

Differential Regulation of Prelimbic and Thalamic Transmission to the Basolateral Amygdala by Acetylcholine Receptors.

Applications

Unspecified application

Species

Unspecified reactive species

Sarah C Tryon,Joshua X Bratsch-Prince,James W Warren,Grace C Jones,Alexander J McDonald,David D Mott

The Journal of surgical research 244:358-367 PubMed31323391

2019

M1 Macrophage Activated by Notch Signal Pathway Contributed to Ventilator-Induced Lung Injury in Chronic Obstructive Pulmonary Disease Model.

Applications

Unspecified application

Species

Unspecified reactive species

Hongping Huang,Hui Feng,Dong Zhuge

The Journal of neuroscience : the official journal 37:2292-2304 PubMed28137966

2017

Loss of M1 Receptor Dependent Cholinergic Excitation Contributes to mPFC Deactivation in Neuropathic Pain.

Applications

Unspecified application

Species

Unspecified reactive species

Daniel Radzicki,Sarah L Pollema-Mays,Antonio Sanz-Clemente,Marco Martina

Anesthesia and analgesia 124:1330-1338 PubMed28002166

2016

The Analgesic Effects of (5R,6R)6-(3-Propylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo[3.2.1] Octane on a Mouse Model of Neuropathic Pain.

Applications

Unspecified application

Species

Unspecified reactive species

Yong-Jie Wang,Zhen-Xing Zuo,Mei Zhang,Zhi-Hui Feng,Min Yan,Xiang-Yao Li
View all publications

Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com